» Articles » PMID: 35651749

Influence of DNA Extraction Kits on Freshwater Fungal DNA Metabarcoding

Overview
Journal PeerJ
Date 2022 Jun 2
PMID 35651749
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Environmental DNA (eDNA) metabarcoding is a common technique for efficient biodiversity monitoring, especially of microbes. Recently, the usefulness of aquatic eDNA in monitoring the diversity of both terrestrial and aquatic fungi has been suggested. In eDNA studies, different experimental factors, such as DNA extraction kits or methods, can affect the subsequent analyses and the results of DNA metabarcoding. However, few methodological studies have been carried out on eDNA of fungi, and little is known about how experimental procedures can affect the results of biodiversity analysis. In this study, we focused on the effect of DNA extraction method on fungal DNA metabarcoding using freshwater samples obtained from rivers and lakes.

Methods: DNA was extracted from freshwater samples using the DNeasy PowerSoil kit, which is mainly used to extractmicrobial DNA from soil, and the DNeasy Blood & Tissue kit, which is commonly used for eDNA studies on animals. We then compared PCR inhibition and fungal DNA metabarcoding results; operational taxonomic unit (OTU) number and composition of the extracted samples.

Results: No PCR inhibition was detected in any of the samples, and no significant differences in the number of OTUs and OTU compositions were detected between the samples processed using different kits. These results indicate that both DNA extraction kits may provide similar diversity results for the river and lake samples evaluated in this study. Therefore, it may be possible to evaluate the diversity of fungi using a unified experimental method, even with samples obtained for diversity studies on other taxa such as those of animals.

Citing Articles

The Use of eDNA Metabarcoding to Detect and Identify Phytophthora in Water Samples.

Randall E, Keillor B, Cooke D Methods Mol Biol. 2024; 2892:117-138.

PMID: 39729273 DOI: 10.1007/978-1-0716-4330-3_9.

References
1.
Doi H, Fukaya K, Oka S, Sato K, Kondoh M, Miya M . Evaluation of detection probabilities at the water-filtering and initial PCR steps in environmental DNA metabarcoding using a multispecies site occupancy model. Sci Rep. 2019; 9(1):3581. PMC: 6401178. DOI: 10.1038/s41598-019-40233-1. View

2.
Grossart H, Van den Wyngaert S, Kagami M, Wurzbacher C, Cunliffe M, Rojas-Jimenez K . Fungi in aquatic ecosystems. Nat Rev Microbiol. 2019; 17(6):339-354. DOI: 10.1038/s41579-019-0175-8. View

3.
Takasaki K, Aihara H, Imanaka T, Matsudaira T, Tsukahara K, Usui A . Water pre-filtration methods to improve environmental DNA detection by real-time PCR and metabarcoding. PLoS One. 2021; 16(5):e0250162. PMC: 8104373. DOI: 10.1371/journal.pone.0250162. View

4.
Fujii K, Doi H, Matsuoka S, Nagano M, Sato H, Yamanaka H . Environmental DNA metabarcoding for fish community analysis in backwater lakes: A comparison of capture methods. PLoS One. 2019; 14(1):e0210357. PMC: 6354990. DOI: 10.1371/journal.pone.0210357. View

5.
Hartman L, Coyne S, Norwood D . Development of a novel internal positive control for Taqman based assays. Mol Cell Probes. 2005; 19(1):51-9. DOI: 10.1016/j.mcp.2004.07.006. View